Inactivation of Native K Channels

J Membr Biol. 2022 Feb;255(1):13-31. doi: 10.1007/s00232-021-00195-w. Epub 2021 Aug 12.

Abstract

We have experimented with isolated cardiomyocytes of mollusks Helix. During the whole-cell patch-clamp recordings of K+ currents a considerable decrease in amplitude was observed upon repeated voltage steps at 0.96 Hz. For these experiments, ventricular cells were depolarized to identical + 20 mV from a holding potential of - 50 mV. The observed spontaneous inhibition of outward currents persisted in the presence of 4-aminopyridine, tetraethylammonium chloride or E-4031, the selective class III antiarrhythmic agent that blocks HERG channels. Similar tendency was retained when components of currents sensitive to either 4-AP or TEA were mathematically subtracted. Waveforms of currents sensitive to 1 and 10 micromolar concentration of E-4031 were distinct comprising prevailingly those activated during up to 200 ms pulses. The outward current activated by a voltage ramp at 60 mV x s-1 rate revealed an inward rectification around + 20 mV. This feature closely resembles those of the mammalian cardiac delayed rectifier IKr.

Keywords: Heart; Helix; Inactivation; K+ currents; Mollusk; Tail.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Aminopyridine* / pharmacology
  • Animals
  • In Vitro Techniques
  • Mammals
  • Membrane Potentials
  • Patch-Clamp Techniques
  • Potassium Channels*
  • Tetraethylammonium / pharmacology

Substances

  • Potassium Channels
  • Tetraethylammonium
  • 4-Aminopyridine